Augui S, Filion G J, Huart S, Nora E, Guggiari M, Maresca M, Stewart A F, Heard E
CNRS UMR218, Curie Institute, 26 rue d'Ulm, Paris 75005, France.
Science. 2007 Dec 7;318(5856):1632-6. doi: 10.1126/science.1149420.
Mammalian dosage compensation involves silencing of one of the two X chromosomes in females and is controlled by the X-inactivation center (Xic). The Xic, which includes Xist and its antisense transcription unit Tsix/Xite, somehow senses the number of X chromosomes and triggers Xist up-regulation from one of the two X chromosomes in females. We found that a segment of the mouse Xic lying several hundred kilobases upstream of Xist brings the two Xics together before the onset of X inactivation. This region can autonomously drive Xic trans-interactions even as an ectopic single-copy transgene. Its introduction into male embryonic stem cells is strongly selected against, consistent with a possible role in trans-activating Xist. We propose that homologous associations driven by this novel X-pairing region (Xpr) of the Xic enable a cell to sense that more than one X chromosome is present and coordinate reciprocal Xist/Tsix expression.
哺乳动物的剂量补偿涉及雌性两条X染色体中的一条失活,并由X染色体失活中心(Xic)控制。Xic包括Xist及其反义转录单元Tsix/Xite,它以某种方式感知X染色体的数量,并触发雌性两条X染色体之一上的Xist上调。我们发现,位于Xist上游数百千碱基处的一段小鼠Xic在X染色体失活开始前将两个Xic聚集在一起。即使作为异位单拷贝转基因,该区域也能自主驱动Xic的反式相互作用。将其引入雄性胚胎干细胞会受到强烈的选择抑制,这与它在反式激活Xist中的可能作用一致。我们提出,由Xic的这个新的X配对区域(Xpr)驱动的同源关联使细胞能够感知存在不止一条X染色体,并协调Xist/Tsix的相互表达。